• No results found

Antibiotic treatment and length of hospital stay in relation to delivery mode and prematurity

N/A
N/A
Protected

Academic year: 2023

Share "Antibiotic treatment and length of hospital stay in relation to delivery mode and prematurity"

Copied!
14
0
0

Loading.... (view fulltext now)

Full text

(1)

http://openarchive.ki.se

This is a Peer Reviewed Published version of the following article, accepted for publication in PLoS One.

2017-01-02

Antibiotic treatment and length of hospital stay in relation to delivery mode and prematurity

Ahlén, Katia M.; Örtqvist, Anne K.; Gong, Tong; Wallas, Alva K.; Ye, Weimin; Lundholm, Cecilia; Almqvist, Catarina

PLoS One. 2016 Oct 7;11(10):e0164126.

Public Library of Science

http://doi.org/10.1371/journal.pone.0164126 http://hdl.handle.net/10616/45475

If not otherwise stated by the Publisher's Terms and conditions, the manuscript is deposited under the terms of the Creative Commons Attribution-NonCommercial-NoDerivatives License (http://creativecommons.org/licenses/by-nc-nd/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited, and is not altered, transformed, or built upon in any way.

(2)

Antibiotic Treatment and Length of Hospital Stay in Relation to Delivery Mode and

Prematurity

Katia M. Ahle´n1*, Anne K. O¨ rtqvist1, Tong Gong1, Alva Wallas2, Weimin Ye1, Cecilia Lundholm1, Catarina Almqvist1,3

1 Dept of Medical Epidemiology and Biostatistics, Karolinska Institutet, Stockholm, Sweden, 2 Institute of Environmental Medicine, Karolinska Institutet, Stockholm, Sweden, 3 Astrid Lindgren Children’s Hospital, Lung and Allergy Unit, Karolinska University Hospital, Stockholm, Sweden

*katia.ahlen@gmail.com

Abstract

Aim

To investigate how 1) maternal delivery mode and 2) prematurity in infants are associated to antibiotic treatment and length of hospital stay.

Methods

Women having given birth and infants 0–12 months discharged from hospital between July 2005 and November 2011 were identified from the Swedish National Patient Register. Med- ical records were reviewed for 203 women and 527 infants. The risk ratio (RR) between antibiotic treatment and 1) delivery mode in women; 2) prematurity in infants was calcu- lated. Length of stay and days of antibiotic therapy were compared by Wilcoxon rank-sum test.

Results

Women: There was an association between emergency caesarean section (CS) and antibi- otic treatment (RR 5.0 95% confidence interval (CI) 2.2–11.5), but not for elective CS.

Length of stay was longer for CS (emergency and elective) compared to vaginal delivery (p<0.01). Infants: RR for antibiotic treatment in preterm compared to term infants was 1.4 (95% CI 1.0–1.9). Length of stay (p<0.01), but not days of therapy (p = 0.17), was higher in preterm compared to term infants.

Conclusion

We found that emergency CS increased the probability of maternal antibiotic treatment dur- ing hospitalisation, but no difference was found between term and preterm infants. The results are well aligned with current guidelines and may be considered in future studies on the effects of antibiotics.

a11111

OPEN ACCESS

Citation: Ahle´n KM, O¨ rtqvist AK, Gong T, Wallas A, Ye W, Lundholm C, et al. (2016) Antibiotic Treatment and Length of Hospital Stay in Relation to Delivery Mode and Prematurity. PLoS ONE 11 (10): e0164126. doi:10.1371/journal.

pone.0164126

Editor: Tailoi Chan-Ling, University of Sydney, AUSTRALIA

Received: February 25, 2016 Accepted: September 20, 2016 Published: October 7, 2016

Copyright:© 2016 Ahle´n et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

Data Availability Statement: The authors confirm that, for approved reasons, some access restrictions apply to the data underlying the findings. Data is available from third party; the Swedish National Board of Health and Welfare.

According to Swedish law, the authors are not able to share the register data used in this study with other researchers. Any researcher interested in obtaining the data used can do so by formally applying to the Swedish National Board of Health and Welfare and Statistics Sweden after obtaining an ethical permission from a Regional Ethical

(3)

Introduction

Antibiotics are commonly used worldwide to treat bacterial infections in children and adults.

In Sweden, one of three patients receive antibiotics during hospitalisation and hospitals account for 11% of the total national antibiotic use [1]. Information on dispensed antibiotics at an individual level in outpatient care is available through the Swedish Prescribed Drug register (SPDR) [2], but there is no equivalent register for inpatient care. Thus, information on the full individual exposure to antibiotics is currently unavailable. Although antibiotics are essential for treating serious bacterial infections, extensive use promotes antibiotic resistance and trans- mission of nosocomial infections [1]. Antibiotics given to the mother peri-partum may affect the pattern of infection in the child after birth [3] and early life exposure to antibiotics has been suggested to affect the colonisation of the gut flora and the developing immune system [3,4].

Long term health consequences that have been linked to antibiotic exposure during fetal and early life include obesity [5,6], allergic disease [7,8] and asthma [8,9]. However, further stud- ies are needed to understand the causality and potential confounders affecting these associa- tions [10,11].

The average length of stay in Swedish hospitals for women giving birth was 2.2 days for vag- inal delivery (VD) and 3.7 days for cesarean section (CS) in 2009 [12]. A survey of clinical guidelines in Swedish obstetric clinics showed that most clinics recommend antibiotic prophy- laxis for emergency CS (which holds a higher risk of maternal post-partum infection), but not for elective CS [13]. Antibiotic prophylaxis is used during VD if risk factors for vertical trans- mission of Group B- Streptococci exist or in pre-labour premature rupture of membranes (pPROM) in week 22–32, to reduce risk of chorioamnionitis and neonatal infection [14]. Apart from the knowledge of current guidelines, we are not aware of any previous study that has investigated the relation between different delivery modes and the probability of antibiotic treatment in mothers giving birth

Bacterial infections in infants often present with unspecific symptoms and are difficult to diagnose, which may lead to both over-treatment and under-treatment with antibiotics [15].

Neonates with clinical symptoms of sepsis are commonly given empirical antibiotic treatment before confirmation of bacterial origin to prevent mortality in neonatal sepsis [16]. Preterm infants have a less developed innate immune system than term infants, with an increased risk for bacterial infections [17]. Furthermore, since maternal infection is one important mecha- nism contributing to spontaneous preterm births, preterm infants are more likely to be exposed to pathogens intra-uterine [18]. Preterm infants also have an increased length of stay compared to term infants [19] and are more often exposed to invasive medical devices during hospitaliza- tion [17], which increases the risk of nosocomial infections. Thus, it is likely that preterm infants are treated with antibiotics more frequently than term infants. Previous point preva- lence studies have reported on general antibiotic use in inpatient care on a national level [20, 21] and we have recently reported proportions of antibiotics treatment with different child- hood and maternal diagnoses [22], but comparisons between term and preterm birth have not been performed.

Since antibiotics given during the fetal and early life may affect the infant’s future health, it is of importance to study how pregnant women and infants are exposed to antibiotics in hospi- tals in addition to the available information from outpatient care. The aim of this study was to investigate the association between inpatient antibiotic treatment and delivery mode in preg- nant women and prematurity in infants. Moreover, we aimed to examine how length of stay and days of therapy differed between the groups.

Review board in Sweden. The Swedish National Board of Health and Welfare can be contacted at:

Socialstyrelsen 106 30 Stockholm +46752473000 socialstyrelsen@socialstyrelsen.se.

Funding: This work was supported by the grants from a) the Swedish Research Council (Vetenskapsrådet) Grant number 2011-3060 (http://www.vr.se/) to CA; b) the Swedish Initiative for Research on Microdata in the Social And Medical Sciences Grants no 80748301 and 340- 2013-5867) (http://simsam.nu/) to CA and WY; c) Stockholm County Council (Stockholms La¨ns Landsting) ALF-projects award numbers 502262, 520344 and 530422 (http://www.sll.se/) to CA; d) the Strategic Research Program in Epidemiology at Karolinska Institutet (www.ki.se) to CA; e) the Swedish Heart-Lung Foundation (https://www.

hjart-lungfonden.se/) to CA. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.

Competing Interests: The authors have declared that no competing interests exist.

(4)

Patients and methods Study design and population

This cross-sectional population-based study was based on linkage between registers held by the National Board of Health and Welfare (NBHW); SPDR, the National Patient Register (NPR) and the Medical Birth Register (MBR). The Swedish Personal Identity Number (PIN) is a unique identifier for every resident in Sweden and enables linkage of registers. SPDR contains information on all prescribed drugs in outpatient care since July 2005, classified according to the Anatomical Therapeutic Chemical classifications system (ATC). NPR contains national information on all primary and secondary diagnoses in inpatient care since 1987. MBR was established in 1973 and includes data on more than 98% of all births in Sweden.

In 2011, a linkage between the NPR and SPDR was performed at the NBHW and a cohort of all pregnant women and all children 0–5 years with a discharge date in the NPR between 1st July 2005 and 30th of November 2011 were identified as previously described (24). In this pres- ent study three groups were selected from the initial cohort for further study, according to patient’s age and diagnosis in NPR; 1) women with a diagnosis of VD (according to the Inter- national Classification of Disease, 10threvision (ICD-10): O80), elective CS (O82.0) or emer- gency CS (O82.1); 2) infants aged 0–12 months at discharge with a primary or secondary diagnosis of prematurity (ICD-10: P07.2 or P07.3) and 3) infants aged 0–12 months without a diagnosis of prematurity (i.e. term infants). Pregnancy was defined as the period between the estimated date of conception and the infants’ birth date, based on information on gestational age fromMBR. Term infants with a primary diagnosis of malformations or factors influencing health status (ICD-10 codes Q or Z) were excluded to obtain a healthy reference group. A ran- dom sample of hospital visits from each group (n = 250 women, n = 640 infants) were drawn by the NBHW and the patient’s PIN’s were provided. In order to target patients who were given antibiotics only during the hospitalisation, individuals with a dispensed prescription of antibiotics in SPDR at the same day or day after the discharge date in NPR were excluded.

Requested medical records

Starting in January 2012, the study participants’ medical records, corresponding to the date of discharge and PIN, were requested by a letter to the head of the ward where the patient had been treated. Two reminder letters were sent out before the end of data collection in June 2013.

Each medical record was manually reviewed and all available information regarding diagnosis, length of stay and potential antibiotic treatment was extracted. The numbers of requested and received medical records and the final study populations of women and infants are displayed in Figs1and2. In total, medical records were received for 222 hospital visits for women and 546 hospital visits for infants, which correspond to a response rate of 89% and 85% respec- tively. Furthermore, thirty-eight hospital visits (19 women and 19 infants) were excluded due to missing information on antibiotic use, resulting in a final study population of 203 hospital visits for women and 527 hospital visits for infants.

Variables

Information on women’s and infants’ age at admission and infants’ sex was extracted from the medical records. In women, age 30–34 years was chosen as reference group since it constituted the majority of individuals. Preterm infants were categorised as moderately preterm (born between 28–36 completed gestational weeks, ICD-10: P07.3) and extremely preterm (born before 28 completed gestational weeks, ICD-10: P07.2). Infant age was categorized as <3 months, 3–5, 6–8 and 9–12 months. Length of stay was defined as the period between date of

(5)

Fig 1. Study population and medical record request for pregnant women. Medical records were randomly selected from a register-based cohort of patients treated in Swedish hospitals between July 2005 and November 2011. Abbreviations: NPR = National Patient Register, MBR = Medical Birth Register, SPDR = Swedish Prescribed Drug Register, ICD-10 = International Classification of Disease 10threvision.

doi:10.1371/journal.pone.0164126.g001

(6)

admission and discharge. Administration of antibiotics was identified in the medical records by ATC-code J01. Antibiotic treatment was categorised as “yes”, if antibiotics were adminis- tered at any time during hospitalisation; “no” if antibiotics were not given. “Days of therapy”

Fig 2. Study population and medical record request for infants 0–12 months. Medical records were randomly selected from a register-based cohort of patients treated in Swedish hospitals between July 2005 and November 2011. Abbreviations: NPR = National Patient Register, SPDR = Swedish Prescribed Drug Register, ICD-10 = International Classification of Disease 10threvision.

doi:10.1371/journal.pone.0164126.g002

(7)

was defined as the total number of days with any or multiple types of antibiotic treatment. For each individual, treatment days for all administrations of antibiotics were summed. Individuals with missing information on both start- and end date, were excluded from the analysis on days of therapy. If information was missing only for the end date, treatment time for each adminis- tration was assumed to be one day. Information on start- and end date was complete only in half of the women treated with antibiotics. Thus, the analysis of days of therapy was only per- formed among infants.

Statistical analysis

Risk ratio (RR) with 95% confidence intervals (CI) were estimated for antibiotic treatment in relation to delivery mode and degree of prematurity, according to Cornfield [23]. Since the age distribution of infants differed considerably between term and preterm infants, sub-analyses were performed for the age category with the majority of individuals (0–3 months). Descriptive statistics for length of stay (all individuals) and days of therapy (infants with antibiotic treat- ment in medical records) were presented in a box plot. Due to skewed distributions, two-sam- ple Wilcoxon rank-sum test was used for comparisons between groups for length of stay and days of therapy. Cuzick’s non-parametric test for trend [24] was used to investigate the dose- response relationship for “term”, “moderately preterm”, and “extremely preterm” infants in relation to antibiotic treatment, length of stay and days of therapy. Significance was set at the 5% level. All analyses were performed using Stata statistical software, version 12.

Ethical considerations

Consent to access the medical records was given by the head of each medical department. All data extracted from the medical records was de-identified prior to analysis and is presented in an aggregated way where no results may be connected to specific patients. The study has been approved by the Regional Ethical Review Board in Stockholm, Sweden.

Results

Pregnant women

Table 1displays antibiotic treatment in relation to delivery mode and age at delivery in preg- nant women (N = 203). Almost two out of three women who gave birth with emergency CS (63%) were treated with antibiotics, while less than one in seven women who gave birth by elec- tive CS (14%) or VD (13%) received antibiotics. Women delivering by emergency CS were thus five times more likely to receive antibiotics compared to women delivering by VD (RR 5.0, 95%

CI 2.2–11.5), but no significant difference was found when comparing elective CS to VD. The proportion of women treated with antibiotics in relation to maternal age at delivery varied between 34% (25–29 years) and 47% (<25 years). However, the difference between age groups was not statistically significant. Length of stay was significantly higher for both emergency and elective CS compared to VD (p<0.01) (Fig 3).

Infants

The youngest age group (< 3 months) contained a majority of the infants in the study popula- tion (55% of the term and 92% of the preterm infants). The number of individuals in each of the age groups 3–5, 6–8 and 9–12 months decreased with increasing age. The majority of both term (61%) and preterm (59%) infants in the study population were males (data not tabulated).

Table 2presents antibiotic treatment in infants in relation to prematurity, sex and age at admis- sion. In total, 22% of all infants were treated with antibiotics at least once during

(8)

hospitalisation. RR for antibiotic treatment in preterm compared to term infants was 1.4, but the results did not reach statistical significance (95% CI 1.0–1.9). However, extremely preterm infants were twice as likely to receive antibiotics compared to term infants (RR 2.4, 95% CI 1.5–3.7) and there was a significant dose-response relationship for “term”, “moderately pre- term”, and “extremely preterm” infants in relation to antibiotic treatment (p<0.01). There was no statistically significant association between antibiotic treatment and sex or age among term

Table 1. Risk ratios (RR) and 95% confidence intervals (CI) for antibiotic treatment in relation to delivery mode and maternal age at delivery (N = 203).

All Antibiotics

N No, n (%) Yes, n (%) RR (95% CI)

Delivery mode Vaginal 40 35 (87.5) 5 (12.5) 1 (ref)

Elective CS 64 55 (85.9) 9 (14.1) 1.1 (0.4–3.1)

Emergency CS 99 37 (37.4) 62 (62.6) 5.0 (2.2–11.5)

Age (years) <25 17 9 (52.9) 8 (47.1) 1.3 (0.7–2.3)

25–29 47 31 (66.0) 16 (34.0) 0.9 (0.6–1.5)

30–34 74 47 (63.5) 27 (36.5) 1 (ref)

>35 65 40 (61.5) 25 (38.5) 1.05 (0.7–1.6)

doi:10.1371/journal.pone.0164126.t001

Fig 3. Boxplot with mean (◆) for length of stay for women by delivery mode. For elective CS, the median is equal to the lower quartile.

Abbreviations: CS = Caesarean section

doi:10.1371/journal.pone.0164126.g003

(9)

or preterm infants. Sub-analyses of antibiotic treatment in infants 0–3 months showed similar results as in the entire study population, with a small but not statistically significant difference between term and preterm infants (RR 1.2, 95% CI 0.8–1.8) and a doubled probability of anti- biotic treatment in extremely preterm infants (RR 2.6, 95% CI 1.6–4.2) (S1 Table).

Fig 4displays the distribution of length of stay and days of therapy for term, moderately pre- term and extremely preterm infants. Length of stay was significantly higher in both moderately and extremely preterm infants compared to term infants (p<0.01), and showed a significant dose-response relationship (p<0.01). To calculate days of therapy for infants who had received antibiotics (n = 118), individuals with missing information on start- and end date were excluded (n = 9). Analysis was performed for the remaining 109 individuals and included 20 individuals (18.3%) where end date was missing and treatment time had been assumed to be one day. The median for days of therapy was 5 days for both preterm and term infants. No dif- ference in days of therapy was found between term and preterm infants, neither when treating prematurity as dichotomous (Wilcoxon rank sum test, p = 0.17) or with degree of prematurity (Cuzick’s trend test, p = 0.30).

Discussion

We found that women who delivered by emergency CS were five times more likely to receive antibiotics compared to women who delivered by VD or elective CS. Length of stay was signifi- cantly higher in women who delivered by CS compared to VD. Although antibiotic treatment in preterm infants overall did not reach statistical significance compared to term infants, extremely preterm infants were twice as likely to receive treatment as term infants. Length of stay was significantly higher in preterm infants compared to term infants, but no difference could be seen in days of therapy.

The prevalence of maternal antibiotic administration peri-partum varies globally. Global surveys performed in non-European countries by the World Health Organisation reported that antibiotics were administered to 47% of VD [25] and 87% of elective and emergency CS [26]. A Danish cohort study of 750 women found that antibiotics were given to 13% of VD and that antibiotic prophylaxis was given to all CS [27]. Several countries, such as Canada [28] and the United Kingdom [29], have implemented national guidelines recommending antibiotic pro- phylaxis for both elective and emergency CS. In contrast, our results from Swedish medical rec- ords suggest that antibiotics are commonly used in emergency CS but not as often in elective

Table 2. Risk ratios (RR) and 95% confidence intervals (CI) for antibiotic treatment by prematurity, sex and age in infants 0–12 months of age.

All Antibiotics

N No, n (%) Yes, n (%) RR (95% CI)

All 527 409 (77.6) 118 (22.4) -

Prematurity Term 259 210 (81.1) 49 (18.9) 1 (ref)

Preterm 268 199 (74.2) 69 (25.8) 1.4 (1.0–1.9)

Moderately 230 178 (77.4) 52 (22.6) 1.2 (0.8–1.7)

Extremely 38 21 (55.3) 17 (44.7) 2.4 (1.5–3.7)

Sex Male 317 251 (79.2) 66 (20.8) 1 (ref)

Female 210 158 (75.2) 52 (24.8) 1.2 (0.9–1.6)

Age (months) <3 389 295 (75.8) 94 (24.2) 1 (ref)

3–5 64 53 (82.8) 11 (17.2) 0.7 (0.4–1.3)

6–8 42 35 (83.3) 7 (16.7) 0.7 (0.3–1.4)

9–12 32 26 (81.2) 6 (18.8) 0.8 (0.4–1.6)

doi:10.1371/journal.pone.0164126.t002

(10)

CS. This is in concordance with the local clinical guidelines from the Swedish Strategic Pro- gram against Antimicrobial Resistance [14] and a national survey of clinical guidelines [13].

Approximately 22% of the infants in this study received antibiotics during hospitalisation.

Previous point prevalence studies by the Swedish Strategic Program against Antimicrobial Resistance have reported that an average of 29% of children aged 0–16 years were treated with antibiotics during hospitalisation [21]. Since we did not include patients who had a dispensed prescription of antibiotics in SPDR at the same day or day after the discharge, it is reasonable that we report a lower proportion of antibiotic treatment compared to the point prevalence study.

A large part of our study population consisted of neonates. Although neonatal sepsis is a rel- atively uncommon condition (3-4/1000 born children), it can develop rapidly and has a mor- tality of 9–15% [30]. Neonates with clinical symptoms of sepsis are routinely given empirical antibiotic treatment, before confirmation of bacterial origin, in order to prevent mortality.

Fig 4. Boxplot with mean (◆) for length of stay and days of therapy for infants by degree of prematurity. Abbreviations: MP = Moderately premature, EP = Extremely premature

doi:10.1371/journal.pone.0164126.g004

(11)

[16]. Early onset sepsis occurs within 72 hours after birth and the infection is often transmitted vertically by bacteria in the mother’s urogenital tract or intra-amniotic fluid. Late onset sepsis which occurs more than 72 hours after birth is acquired by pathogens in the environment [30].

Antibiotic use among neonates in selected hospitals has previously been described in different prospective cohort studies. For example, Zingg et al found that 26.7% of neonates in Geneva, Switzerland, were treated with antibiotics for an average of 6.8 days [31], while Cantey et al found that 72% of the neonates in Texas, US were treated with antibiotics for an average of 5.7 days [32]. However, neither of the studies addressed differences in antibiotic treatment between term and preterm neonates. Furthermore, due to differences in patient characteristics, level of health care and demographic factors it is difficult to compare results between single- center studies.

In our study, extremely preterm infants were twice as likely to receive antibiotic treatment during hospitalisation compared to term infants, while no significant difference could be seen between moderately preterm and term infants. As a group, extremely preterm infants have very high morbidity; half of surviving infants have been estimated to suffer from severe neona- tal morbidities [33]. In contrast, moderately preterm infants have a health status more like term infants, which could explain the similar results between these moderately preterm and term infants.

Håkansson et al studied antibiotic use in neonatal wards on a national level, through the Swedish Neonatal Quality Register [30]. A strong correlation was seen between days of antibi- otic therapy and gestational age; days of therapy varied between a mean of 1 day of therapy in term infants to 37 days of therapy in the extremely premature infants. In contrast, we did not find a significant difference in days of therapy between term, moderately preterm and extremely preterm individuals. This could be due to the wider range of age our study covered (first year of life compared to the neonatal period) and also that we included antibiotic treat- ment independent of diagnosis, while Håkansson et al focused mainly on infants with neonatal sepsis. We observed a difference in age distribution between term and preterm infants in our study population. This is likely due to the fact that the indications for hospitalisation differ between term and preterm, since a larger proportion of preterm infants are hospitalised in con- nection to birth compared to term infants. Since the difference in age between the two groups could affect our results, sub-analyses were performed for infants 0–3 months. However, the results did not differ compared to the entire study population.

The strength of our study is the initial cohort of women and infants identified from the Swedish nation-wide population-based health registers. Since our cohort included all hospital admissions for the selected diagnoses in Sweden between July 2005 and November 2011, the risk for selection bias is minimised. Furthermore, the response rate of medical records for both groups of women and infants was high, which is important for the results to be representative of the target population. By combining register data with patient data from medical records, we were able to study individual antibiotic treatment in relation to delivery mode and prematurity within hospitals, in a way not previously performed in Sweden.

The study has some limitations. Firstly, we had relatively small sample sizes, resulting in wide confidence intervals. Our results should therefore be interpreted with caution due to pos- sible lack of power. Secondly, the reliability of information about antibiotics in the medical rec- ords could be discussed. Antibiotics were only used in 62% of emergency CS, which is low considering current guidelines. It is possible that antibiotics may have been given in reality, but that it was not stated in the discharge summary or included in the provided drug-record.

Thirdly, the information regarding days of therapy was incomplete on several occasions. Our data included antibiotics given to the woman during the entire time of hospitalisation but due to lack of information on start and end date of antibiotic exposure, we cannot draw any

(12)

conclusions regarding if the antibiotics was given peri-partum or post- partum in this group.

Finally, since preterm infants are at a higher risk of exposure to intra-uterine infection due to chorioamnionitis (34) and pPROM (18) it would have been interesting also to study these con- ditions; however our sample size was too small.

In conclusion, women delivering by emergency CS had a higher probability of treatment with antibiotics than other modes of delivery and all CS had an increased length of stay com- pared to VD. These results confirm current guidelines. Extremely preterm infants were twice as likely to receive antibiotic treatment compared to term infants. Preterm infants overall were not more likely to receive antibiotic treatment, although a dose-response trend could be observed for degree of prematurity. The hospital stay was longer in preterm infants. Since exposure to antibiotics in early life may be linked to long term health consequences, difference in antibiotic treatment between the groups may be taken into consideration in future studies investigating the long term health effects of antibiotic exposure in early life.

Supporting Information

S1 Table. Risk ratios (RR) and 95% confidence intervals (CI) for antibiotic treatment by prematurity, sex and age in infants 0–3 months of age.

(DOCX)

Acknowledgments

We would like to acknowledge Gerd Agerberg and Michael Broms who contributed with excel- lent database management.

Author Contributions

Conceptualization: CA WY.

Formal analysis: AÖ TG AW.

Funding acquisition: CA WY.

Methodology: CA WY AÖ CL.

Project administration: CA AÖ.

Supervision: CL CA.

Writing – original draft: KA AÖ.

Writing – review & editing: KA AÖ CA TG CL AW WY.

References

1. Hellman J, Olsson-Liljeqvist B, Bengtsson B, Greko C, (eds). SWEDRES-SVARM 2012. Solna/Upp- sala: Strama; 2012 [cited 2015 May 8]. Available from:http://www.sva.se/globalassets/redesign2011/

pdf/om_sva/publikationer/swedres_svarm2012.pdf.

2. Wettermark B, Hammar N, Fored CM, Leimanis A, Otterblad Olausson P, Bergman U, et al. The new Swedish Prescribed Drug Register—opportunities for. Pharmacoepidemiol Drug Saf. 2007; 16 (7):726–35. Epub 2006/08/10. doi:10.1002/pds.1294PMID:16897791.

3. Bedford Russell AR, Murch SH. Could peripartum antibiotics have delayed health consequences for the infant? BJOG. 2006; 113(7):758–65. Epub 2006/07/11. doi:10.1111/j.1471-0528.2006.00952.x PMID:16827757.

(13)

4. Sudo N, Sawamura S, Tanaka K, Aiba Y, Kubo C, Koga Y. The requirement of intestinal bacterial flora for the development of an IgE production system fully susceptible to oral tolerance induction. J Immu- nol. 1997; 159(4):1739–45. Epub 1997/08/15. PMID:9257835.

5. Trasande L, Blustein J, Liu M, Corwin E, Cox LM, Blaser MJ. Infant antibiotic exposures and early-life body mass. Int J Obes (Lond). 2013; 37(1):16–23. Epub 2012/08/22. doi:10.1038/ijo.2012.132PMID:

22907693; PubMed Central PMCID: PMCPmc3798029.

6. Azad MB, Bridgman SL, Becker AB, Kozyrskyj AL. Infant antibiotic exposure and the development of childhood overweight and central adiposity. Int J Obes (Lond). 2014; 38(10):1290–8. Epub 2014/07/

12. doi:10.1038/ijo.2014.119PMID:25012772.

7. Tsakok T, McKeever TM, Yeo L, Flohr C. Does early life exposure to antibiotics increase the risk of eczema? A systematic review. Br J Dermatol. 2013. Epub 2013/06/21. doi:10.1111/bjd.12476PMID:

23782060.

8. Kummeling I, Stelma FF, Dagnelie PC, Snijders BE, Penders J, Huber M, et al. Early life exposure to antibiotics and the subsequent development of eczema, wheeze, and allergic sensitization in the first 2 years of life: the KOALA Birth Cohort Study. Pediatrics. 2007; 119(1):e225–31. Epub 2007/01/04. doi:

10.1542/peds.2006-0896PMID:17200248.

9. Stensballe LG, Simonsen J, Jensen SM, Bonnelykke K, Bisgaard H. Use of antibiotics during preg- nancy increases the risk of asthma in early. J Pediatr. 2013; 162(4):832–8.e3. Epub 2012/11/13. doi:

10.1016/j.jpeds.2012.09.049PMID:23140881.

10. Almqvist C, Wettermark B, Hedlin G, Ye W, Lundholm C. Antibiotics and asthma medication in a large register-based cohort study—confounding, cause and effect. Clin Exp Allergy. 2012; 42(1):104–11.

Epub 2011/11/19. doi:10.1111/j.1365-2222.2011.03850.xPMID:22092483.

11. Ortqvist AK, Lundholm C, Kieler H, Ludvigsson JF, Fall T, Ye W, et al. Antibiotics in fetal and early life and subsequent childhood asthma: nationwide population based study with sibling analysis. Bmj.

2014; 349:g6979. Epub 2014/11/30. doi:10.1136/bmj.g6979PMID:25432937; PubMed Central PMCID: PMCPmc4247260.

12. Graviditeter, fo¨rlossningar och nyfo¨dda barn: medicinska fo¨delseregistrer 1973–2011, assisterad befruktning 1991–2010: Socialstyrelsen; 2013 [cited 2015 May 8]. Available from:http://www.

socialstyrelsen.se/Lists/Artikelkatalog/Attachments/19033/2013-3-27.pdf.

13. Antibiotikaprofylax vid kirurgiska ingrepp: en systematisk litteraturo¨versikt. Stockholm: Statens beredning fo¨r medicinsk utva¨rdering (SBU); 2010 [cited 2015 May 8]. Available from:http://www.sbu.

se/upload/Publikationer/Content0/1/Antibiotikaprofylax_fulltext.pdf.

14. Bergstro¨m M. Antibiotikaanva¨ndning i slutenvård och sa¨rskilda boendeformer- Infektioner inom obste- trik [Internet]: Strama Stockholm; [updated 2013 Aug 28; cited 2015 May 8]. Available from:http://

www.janusinfo.se/Documents/Strama/Slutenv%c3%a5rd/2013/slutenv_obstetrik_2013.pdf.

15. Byington CL, Enriquez FR, Hoff C, Tuohy R, Taggart EW, Hillyard DR, et al. Serious bacterial infec- tions in febrile infants 1 to 90 days old with and without viral infections. Pediatrics. 2004; 113(6):1662–

6. Epub 2004/06/03. doi:10.1542/peds.113.6.1662PMID:15173488.

16. Shane AL, Stoll BJ. Recent developments and current issues in the epidemiology, diagnosis, and man- agement of bacterial and fungal neonatal sepsis. Am J Perinatol. 2013; 30(2):131–41. Epub 2013/01/

09. doi:10.1055/s-0032-1333413PMID:23297182.

17. Sharma AA, Jen R, Butler A, Lavoie PM. The developing human preterm neonatal immune system: a case for more research in this area. Clin Immunol. 2012; 145(1):61–8. Epub 2012/08/29. doi:10.1016/

j.clim.2012.08.006PMID:22926079.

18. Goldenberg RL, Culhane JF, Iams JD, Romero R. Epidemiology and causes of preterm birth. Lancet.

2008; 371(9606):75–84. Epub 2008/01/08. doi:10.1016/s0140-6736(08)60074-4PMID:18177778.

19. Ringborg A, Berg J, Norman M, Westgren M, Jonsson B. Preterm birth in Sweden: what are the aver- age lengths of hospital stay and the associated inpatient costs? Acta Paediatr. 2006; 95(12):1550–5.

Epub 2006/11/30. doi:10.1080/08035250600778636PMID:17129960.

20. Kimland E, Nydert P, Odlind V, Bottiger Y, Lindemalm S. Paediatric drug use with focus on off-label prescriptions at Swedish hospitals—a nationwide study. Acta Paediatr. 2012; 101(7):772–8. Epub 2012/03/13. doi:10.1111/j.1651-2227.2012.02656.xPMID:22404126; PubMed Central PMCID:

PMC3437470.

21. Erntell M, Skoog G, Cars O, Eriksson M, Ska¨rlund K, Elowson S, et al. Point prevalence study of antibi- otic use in hospitalised pediatric patients in Sweden [Internet]: Strama, SMI; 2004 [updated 2004; cited 2015 May 8]. Available from:http://soapimg.icecube.snowfall.se/strama/Poster_SSAC_2004_barn.

ppt.

22. Almqvist C, Ortqvist AK, Gong T, Wallas A, Ahlen KM, Ye W, et al. Individual maternal and child expo- sure to antibiotics in hospital—a national population-based validation study. Acta Paediatr. 2015; 104 (4):392–5. Epub 2014/12/30. doi:10.1111/apa.12916PMID:25545741.

(14)

23. J C. A statistical problem arising from retrospective studies. Proceedings of the Third Berkeley Sympo- sium. 1956; 4:135–48.

24. Cuzick J. A Wilcoxon-type test for trend. (0277–6715 (Print)).

25. Liabsuetrakul T, Lumbiganon P, Mori R, Gulmezoglu M, Souza JP. A secondary analysis of the WHO Global Survey on Maternal and Perinatal Health for antibiotics used in vaginal deliveries. Int J Gynae- col Obstet. 2014; 124(3):240–3. Epub 2014/01/01. doi:10.1016/j.ijgo.2013.07.039PMID:24373702.

26. Morisaki N, Ganchimeg T, Ota E, Vogel JP, Souza JP, Mori R, et al. Maternal and institutional charac- teristics associated with the administration of prophylactic antibiotics for caesarean section: a second- ary analysis of the World Health Organization Multicountry Survey on Maternal and Newborn Health.

BJOG. 2014; 121 Suppl 1:66–75. Epub 2014/03/20. doi:10.1111/1471-0528.12632PMID:24641537.

27. Stokholm J, Schjorring S, Pedersen L, Bischoff AL, Folsgaard N, Carson CG, et al. Prevalence and predictors of antibiotic administration during pregnancy and birth. PLoS One. 2013; 8(12):e82932.

Epub 2013/12/18. doi:10.1371/journal.pone.0082932PMID:24340068; PubMed Central PMCID:

PMCPmc3858309.

28. van Schalkwyk J, Van Eyk N. Antibiotic prophylaxis in obstetric procedures. J Obstet Gynaecol Can.

2010; 32(9):878–92. Epub 2010/11/06. doi:10.1016/s1701-2163(16)34662-xPMID:21050523.

29. Wee MY, Brown H, Reynolds F. The National Institute of Clinical Excellence (NICE) guidelines for cae- sarean sections: implications for the anaesthetist. Int J Obstet Anesth. 2005; 14(2):147–58. Epub 2005/03/30. doi:10.1016/j.ijoa.2004.09.008PMID:15795149.

30. Håkansson S. Neonatal sepsis-epidemiologi, riskfaktorer och sequelae 2013 [cited 2015 May 8]. Avail- able from:https://lakemedelsverket.se/upload/halso-och-sjukvard/behandlingsrekommendationer/

bakg_dok/Bakgrundsdokument_neonatal%20sepsis_webb.pdf.

31. Zingg W, Pfister R, Posfay-Barbe KM, Huttner B, Touveneau S, Pittet D. Secular trends in antibiotic use among neonates: 2001–2008. Pediatr Infect Dis J. 2011; 30(5):365–70. Epub 2010/11/26. doi:10.

1097/INF.0b013e31820243d3PMID:21099446.

32. Cantey JB, Wozniak PS, Sanchez PJ. Prospective Surveillance of Antibiotic Use in the Neonatal Inten- sive Care Unit: Results from the SCOUT Study. Pediatr Infect Dis J. 2014. Epub 2014/09/06. doi:10.

1097/inf.0000000000000542PMID:25191849.

33. Incidence of and risk factors for neonatal morbidity after active perinatal care: extremely preterm infants study in Sweden (EXPRESS). Acta Paediatr. 2010; 99(7):978–92. Epub 2010/05/12. doi:10.

1111/j.1651-2227.2010.01846.xPMID:20456261.

References

Related documents

One of the most active peptides called CP207 (NH2-KWKSFIKKLTSVLKKVVTTAKPLISS-COOH) had good antimicrobial activity against Gram-negative bacteria, high LPS binding affinity

En likhet skulle kunna dras till schackspel där pjäserna rör sig fram, bak och åt sidan (beroende på vilken pjäs det är) under spelets gång. Det som är svårt i dead reckoning

Eftersom Lars Lidgren inte ser att regelverket begränsar honom skulle detta kunna tolkas som att klienternas förväntningar borde vara möjliga att uppfylla och ett

The aim of this study was to describe and explore potential consequences for health-related quality of life, well-being and activity level, of having a certified service or

The aim of this thesis was therefore to explore antibiotic therapy as single treatment of acute appendicitis in unselected adult patients.. A secondary aim was to suggest a

Influence of mode of delivery, family and nursing determinants on early childhood caries development: a prospective cohort study.. Boustedt K, Dahlgren J, Twetman S,

The lower incidence of breastfeeding in infants delivered by C-section probably raises the risk of a less diverse oral microbiota, which can explain the elevated risk of caries

In writing on the men’s work in service occupations, in the context of deindustrialisation, he reports that “Men in my study positively embraced the demands of service work.” (p.